Official recall record

SIGNA Premier systems

US FDA — Medical Devices · 2026-02-27 · United StatesClass II

Issuing authority: US FDA — Medical Devices
Alert date: 2026-02-27
Country of alert: United States
Alert level: Class II
Alert type: recall
Barcode (EAN/GTIN): 00840682135269
Brand on record: GE Healthcare LLC

What the authority reported

Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the magnet rear and if system is accessed to perform service while the magnet is ramped, the magnetic field could attract the ferrous fittings potentially resulting in personnel injury.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: US FDA — Medical Devices · United States · all filters

Same barcode in other registries

The same EAN appears in 1 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

2022-06-24 · US FDA — Medical Devices
SIGNA Premier magnetic resonance scanner, model 5748519.

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.